Canonical Allele Identifier: CA1680243750

Gene: CCR6

Linked Data

• dbSNP Id: rs1781429779

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167112433A>G , CM000668.2:g.167112433A>G	GRCh38
NC_000006.11:g.167525921A>G , CM000668.1:g.167525921A>G	GRCh37
NC_000006.10:g.167445911A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609590.2:n.2170-22501A>G
ENST00000705249.1:c.1066-23605A>G	ENSP00000516101.1:n.1066-23605A>G
ENST00000705250.1:c.844-23605A>G	ENSP00000516102.1:n.844-23605A>G
ENST00000705251.1:c.*713-23605A>G	ENSP00000516103.1:n.*713-23605A>G
ENST00000705252.1:c.*536-23605A>G	ENSP00000516104.1:n.*536-23605A>G
ENST00000705253.1:c.*536-23605A>G	ENSP00000516105.1:n.*536-23605A>G
ENST00000705254.1:c.673-23605A>G	ENSP00000516106.1:n.673-23605A>G
ENST00000705255.1:n.1692-23605A>G
ENST00000400926.5:c.-98+419A>G	ENSP00000383715.2:n.-98+419A>G
NM_004367.5:c.-98+419A>G	NP_004358.2:n.-98+419A>G
XR_943250.1:n.8064T>C
XR_943251.1:n.7483T>C
XR_001744467.2:n.5999T>C
XR_001744469.2:n.5929T>C
XR_943250.3:n.7831T>C
XR_943251.3:n.7491T>C
NM_004367.6:c.-98+419A>G	NP_004358.2:n.-98+419A>G